oculodentodigital dysplasia, autosomal recessive

Preferred Label : oculodentodigital dysplasia, autosomal recessive;

MeSH synonym : oculodentoosseous dysplasia, autosomal recessive;

Origin ID

C567605;

UMLS CUI

C2749477;

Currated CISMeF NLP mapping
- Oculodentodigital dysplasia, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- connexin 43 [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- eye abnormalities [MeSH Descriptor]
- syndactyly [MeSH Descriptor]
- tooth abnormalities [MeSH Descriptor]
Record concept(s)
- oculodentodigital dysplasia, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Oculodentodigital dysplasia, autosomal recessive [OMIM Phenotype]